Effects of cigarette smoke extract on bronchial epithelial cells stimulated with Cryptococcus neoformans.

IF 5.5 3区 医学 Q1 IMMUNOLOGY Medical Microbiology and Immunology Pub Date : 2021-08-01 Epub Date: 2021-07-06 DOI:10.1007/s00430-021-00715-4
Aline Beatriz Mahler Pereira, Jhony Robison Oliveira, Ana Leticia Julio Souza, Leonardo Andrade-Silva, Marcos Vinicius Silva, Paulo Roberto Silva, Mario Leon Silva-Vergara, Alexandre Paula Rogerio
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引用次数: 3

Abstract

In the airways, the adhesion of Cryptococcus neoformans with airway epithelial cells is crucial for the establishment of cryptococcosis. Tobacco smoke is considered a risk factor for cryptococcosis. Here, we evaluated the effects of cigarette smoke extract (CSE) on human bronchial epithelial cells (BEAS-2B) stimulated with C. neoformans. Multiplicities of infection (MOIs) of 1-100 of C. neoformans per cell led to increased IL-8 production and no cytotoxic effects when compared to those of controls. C. neoformans (MOI 100) also significantly increased the concentration of IL-6. In cells stimulated with CSE doses (1.0, 2.5 and 5.0%) from one or five cigarettes, increased IL-1β production was observed only in doses from one (1.0%) and five (2.5%) cigarettes when compared to that of controls. However, only 1.0% CSE failed to show cytotoxic effects. In addition, CSE significantly increased the concentration of IL-8. Cells stimulated with both CSE and C. neoformans demonstrated a reduction in IL-6/STAT3 signalling compared to that in cells stimulated by C. neoformans. In addition, a significant increase in IL-10 production was also observed. No alterations in NF-kB or ICAM-1 expression were observed among the groups. The combination of CSE and C. neoformans favoured the increase of fungal numbers and extracellular adhering of C. neoformans on BEAS-2B cells. In addition, the internalization of C. neoformans on BEAS-2B cells was reduced after CSE stimulation. In conclusion, the association of CSE and C. neoformans induced an anti-inflammatory effect in bronchial epithelial cells, which might favour the development of C. neoformans infection in the airways.

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香烟烟雾提取物对新型隐球菌刺激支气管上皮细胞的影响。
在气道中,新型隐球菌与气道上皮细胞的粘附是隐球菌病形成的关键。吸烟被认为是隐球菌病的一个危险因素。在这里,我们评估了香烟烟雾提取物(CSE)对新生梭状芽胞杆菌刺激的人支气管上皮细胞(BEAS-2B)的影响。与对照组相比,每个细胞感染1-100个新生C.的多重感染(MOIs)导致IL-8的产生增加,但没有细胞毒性作用。C. neoformans (moi100)也显著提高了IL-6的浓度。在1支或5支香烟的CSE剂量(1.0、2.5和5.0%)刺激的细胞中,与对照相比,仅在1支(1.0%)和5支(2.5%)香烟剂量下观察到IL-1β的产生增加。然而,只有1.0%的CSE没有表现出细胞毒性作用。此外,CSE显著提高了IL-8的浓度。与C. neoformans刺激的细胞相比,CSE和C. neoformans刺激的细胞显示IL-6/STAT3信号传导减少。此外,还观察到IL-10产量显著增加。各组间未观察到NF-kB或ICAM-1表达的变化。CSE和新生C. formans联合使用有利于真菌数量的增加和新生C. formans在BEAS-2B细胞上的细胞外粘附。此外,CSE刺激后,新生C. neformans在BEAS-2B细胞上的内化减少。综上所述,CSE和新生梭状菌的关联诱导支气管上皮细胞的抗炎作用,这可能有利于气道新生梭状菌感染的发展。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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